A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800776



Internal ID19160109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57153231..57181418hg38UCSC Ensembl
Innerchr8:58065790..58093977hg19UCSC Ensembl
Innerchr8:58228344..58256531hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3828188
hg1928188
hg1828188
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891399
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800776
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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